Clinical Development


Our laboratory is a certified, independently operating analytical laboratory, providing advanced and sophisticated analytical services with experienced professionals and state-of-the-art instrumentation.

Analysis of active ingredients as such, in blends and finished products such as soft and hard gel caps, tablets and capsules.

Primary packaging - bottling of tablets and capsules.

ACE's up-to-date premises for the manufacturing of clinical trial medication.

Altrabio expertise
Bridge the gap between biologists, statisticians and informaticians.
Outliers and data quality issues
Detect outliers and quality issues that cloud your data.
Life science data analysis and interpretation
Find the needles in your haystack - AltraBio provides expertise in state-of-the-art and innovative life science data analysis and interpretation.
Biomedical knowledge
Place your results in the context of current biomedical knowledge.
New subgroups in your population
Identify new subgroups in your population.

The Analytical Centre of Biopharm, Berlin
The Analytical Centre of Biopharm, Berlin is a German contract research organization providing services on pharmaceutical analysis and bioanalysis for active compounds in the dosage form.
Active compounds stability studies
AZB carries out stability studies in accordance with ICH,including active compounds which are subject to the Addictive Drugs Act.
Quantitative determination of active compounds
AZB has many years of experience in the quantitative determination of active compounds in a biological matrix.
Routine analysis using calibration
Routine analysis is carried out using calibration in the relevant biological matrix, accompanied by a sufficient number of quality control samples.
Determination of physicochemical properties under GLP
Physicochemical properties of intermediates of the chemical industry AZB carries out the determination of physicochemical properties under GLP in accordance with OECD guidelines.

BioAssayLINK global online matching tool
BioAssayLINK is a global online matching tool that provides solutions to your biomedical research and development (R&D) outsourcing/collaboration needs.
BioAssayLINK's interrelated customer groups
BioAssayLINK's interrelated customer groups consist of companies and consultants working in biotechnology, pharmaceuticals, nutraceuticals and biomedical research.
BioAssayLINK's excellent customer service
We provide timely and valuable laboratory and consultant capability options to customers helping them arrive at better decisions more quickly, advancing their R&D objectives.
BioAssayLINK's vision
The company's vision is to be the global online leader linking the services and expertise of specialized laboratries with those individuals, teams and organizations involved in discovery, development and delivery of new healthcare products.
Bioassay matching of animal models of diseas
One of our bioassay matching categories is animal models – animal models of disease, for ADME and toxicology, and spontaneous animal models.

Nucleic acid biomarkers
Array-based technology platforms incorporating novel protein and nucleic acid biomarkers are increasingly being adopted by mainstream diagnostic testing laboratories.
Automated testing platforms
Automated testing platforms are now available for even the most esoteric assays, enabling the adoption of those tests into routine testing laboratories.
Novel biomarkers as diagnostic tests
Biosensor technology is enabling the delivery of diagnostic tests based on novel biomarkers at the point of care.

c-LEcta is located in Leipzig called Bio City
c-LEcta is located in a biotechnology centre in Leipzig called Bio City.
c-LEcta uses state of the art equipment
c-LEcta uses proprietary technologies with state of the art equipment.
c-LEcta runs 600 m² of top equipped lab space
c-LEcta runs 600 m² of top equipped lab space.
c-LEcta’s management team
c-LEcta’s management team is looking forward to discuss the potentials of cooperation with you.
c-LEcta provides almost any desired enzyme activity
c-LEcta develops efficient enzyme production processes based on microbial fermentation.

Contracted immune monitoring services
Contracted immune monitoring services.
Pre-clinical and clinical trial consultation
Pre-clinical and clinical trial consultation.
ELISPOT instrumentation and software
ELISPOT instrumentation and software.
ELISPOT plate scanning and analysis services
ELISPOT plate scanning and analysis services.
PBMC reference samples
PBMC reference samples and serum-free test media.

Europa Bioproducts
Europa Bioproducts specialises in the distribution of enzymes, kits and reagents used in the characterisation and analysis of the glycosylation patterns of therapeutic proteins and monoclonal antibodies.
Post-translational modification
Post-translational modification is important to characterise and monitor because glycosylation has a significant impact on the efficacy, pharmokinetics and safety of the drug.
Oligosaccharide (glycan) profiling and sequencing
Our products allow companies to perform oligosaccharide (glycan) profiling, oligosaccharide (glycan) sequencing and monosaccharide composition.
Signal labelling kits
We have 2-AA (for monosaccharide composition), 2-AB (for oligosaccharide / glycan profiling) and DMB (for sialic acids) Signal labelling kits.
Preliminary identification
Preliminary identification can be achieved by calibrating the column with a 2-AB labelled dextran ladder and comparing retention times to known standards or databases.

FOCUS Clinical Drug Development
FOCUS Clinical Drug Development is an independent full-service CRO that specialises in exploratory clinical drug development and integrated proof of concept (PoC) packages.
FOCUS's Neuss Unit
FOCUS's Neuss Unit has performed >600 Ph I-III studies, more than 80 first-in-man studies (NCE / NBE) and 38 Ph I studies in Japanese subjects since 1997.
FOCUS headquarters
FOCUS headquarters in Neuss, Germany.
Development candidates
FOCUS can progress your development candidate from preclinical / discovery stage to clinical PoC in the most timely and economical fashion, via an integrated project management.
FOCUS Immunology
FOCUS Immunology offers a range of services for exploratory drug development.

Imaging peptides by introducing thioether bridges
LanthioPep increases the in vivo stability of therapeutic and diagnostic imaging peptides by introducing thioether bridges in these peptides.
LanthioPep’s thioether-bridge technology
LanthioPep’s thioether-bridge technology endows peptides with intrinsic in vivo stability thus creating new prospects for unstable peptide drug candidates.
Thioether bridges
LanthioPep has introduced thioether bridges into a broad range of peptides, including peptide hormones and diagnostic imaging peptides.
Stabilised peptide therapeutics and diagnostic imaging candidates
LanthioPep is developing its own stabilised peptide therapeutics and diagnostic imaging candidates.

The Micron Group specialises in clinical research and development
The Micron Group is an international drug development organisation, specialising in clinical research and development.
SILK EDC is a SAS-based suite of software
SILK EDC is a SAS-based suite of software for the capture, management and reporting of data from both clinical studies in phases I to IV and registries.
SILK EDC takes data from both paper and eCRFs
SILK EDC takes data from both paper and eCRFs, but keeps all the advantages of instant access and reporting.
Communications business unit
Our communications business unit produces reports, publications, posters, slidesets and video.
Micron can work globally
Micron can work globally or by continent or country according to the client’s wishes.


Our fifth annual Pharmacovigilance and Risk Management conference will be held 1-2 December 2009 in Brussels, Belgium.
Pharma and biotech manufacturers
The conference will bring together major pharma and biotech manufacturers, as well as regulators, to discuss the important issues of pharmacovigilance and risk management.

This two-day conference will ensure you effectively manage risk management with current medicines to mitigate any risks to patients.


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